Nerol

Nerol is a lipid of Prenol Lipids (PR) class. The involved functions are known as Odorant, Anabolism, Diastasis, Metabolic Inhibition and Oxidation. Nerol often locates in germ tube. The related lipids are Octanols, Pinene, Hexanols, ethyl butyrate and ethyl hexanoate.

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Introduction

To understand associated biological information of Nerol, we collected biological information of abnormalities, associated pathways, cellular/molecular locations, biological functions, related genes/proteins, lipids and common seen animal/experimental models with organized paragraphs from literatures.

What diseases are associated with Nerol?

There are no associated biomedical information in the current reference collection.

No disease MeSH terms mapped to the current reference collection.

PubChem Associated disorders and diseases

What pathways are associated with Nerol

There are no associated biomedical information in the current reference collection.

PubChem Biomolecular Interactions and Pathways

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What cellular locations are associated with Nerol?

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What functions are associated with Nerol?


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What lipids are associated with Nerol?

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What genes are associated with Nerol?

There are no associated biomedical information in the current reference collection.

What common seen animal models are associated with Nerol?

There are no associated biomedical information in the current reference collection.

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All references with Nerol

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Authors Title Published Journal PubMed Link
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Kuwahara Y et al. Geraniol, E-3,7-dimethyl-2,6-octadien-1-ol, as the alarm pheromone of the sycamore lace bug Corythucha ciliata (Say). 2011 J. Chem. Ecol. pmid:22076683
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Shukla M and Dorai K Resolving overlaps in diffusion encoded spectra using band-selective pulses in a 3D BEST-DOSY experiment. 2011 J. Magn. Reson. pmid:21937251
Ahmad ST et al. Preclinical renal cancer chemopreventive efficacy of geraniol by modulation of multiple molecular pathways. 2011 Toxicology pmid:21907755
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Khan MS and Ahmad I In vitro antifungal, anti-elastase and anti-keratinase activity of essential oils of Cinnamomum-, Syzygium- and Cymbopogon-species against Aspergillus fumigatus and Trichophyton rubrum. 2011 Phytomedicine pmid:21893402
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Vinothkumar V and Manoharan S Chemopreventive efficacy of geraniol against 7,12-dimethylbenz[a]anthracene-induced hamster buccal pouch carcinogenesis. 2011 Redox Rep. pmid:21801490
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Katsukawa M et al. Citronellol and geraniol, components of rose oil, activate peroxisome proliferator-activated receptor α and γ and suppress cyclooxygenase-2 expression. 2011 Biosci. Biotechnol. Biochem. pmid:21597168
Merlini V et al. Biomimetic cyclization of geraniol derivatives, a useful tool in the total synthesis of bioactive monocyclic terpenoids. 2011 Nat Prod Commun pmid:21560759
Cruz JC et al. Immobilization of enzymes on fumed silica nanoparticles for applications in nonaqueous media. 2011 Methods Mol. Biol. pmid:21553189
Hisamoto K et al. Hydroxy-group effect on the regioselectivity in a photochemical oxetane formation reaction (the Paternò-Büchi Reaction) of geraniol derivatives. 2011 Photochem. Photobiol. Sci. pmid:21541429
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Szendrei Z et al. Identification and field evaluation of attractants for the cranberry weevil, Anthonomus musculus Say. 2011 J. Chem. Ecol. pmid:21445566
Vieira A et al. Efficacy of geraniol but not of β-ionone or their combination for the chemoprevention of rat colon carcinogenesis. 2011 Braz. J. Med. Biol. Res. pmid:21445532
Marcuzzi A et al. The farnesyltransferase inhibitors tipifarnib and lonafarnib inhibit cytokines secretion in a cellular model of mevalonate kinase deficiency. 2011 Pediatr. Res. pmid:21430599
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Weldon PJ et al. Anointing chemicals and hematophagous arthropods: responses by ticks and mosquitoes to citrus (Rutaceae) peel exudates and monoterpene components. 2011 J. Chem. Ecol. pmid:21409496
Kim SH et al. Geraniol inhibits prostate cancer growth by targeting cell cycle and apoptosis pathways. 2011 Biochem. Biophys. Res. Commun. pmid:21371438
Soh Z et al. An artificial neural network approach for glomerular activity pattern prediction using the graph kernel method and the gaussian mixture functions. 2011 Chem. Senses pmid:21343242
Messaoud C and Boussaid M Myrtus communis berry color morphs: a comparative analysis of essential oils, fatty acids, phenolic compounds, and antioxidant activities. 2011 Chem. Biodivers. pmid:21337502
Aiemsaard J et al. The effect of lemongrass oil and its major components on clinical isolate mastitis pathogens and their mechanisms of action on Staphylococcus aureus DMST 4745. 2011 Res. Vet. Sci. pmid:21316719